Bicyclic (galacto)nojirimycin analogues as glycosidase inhibitors: Effect of structural modifications in their pharmacological chaperone potential towards β-glucocerebrosidase-Reference-Cited by-同舟云学术

Bicyclic (galacto)nojirimycin analogues as glycosidase inhibitors: Effect of structural modifications in their pharmacological chaperone potential towards β-glucocerebrosidase

Published:2011 Issue:10 Volume:9 Page:3698
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Aguilar-Moncayo Matilde,García-Moreno M. Isabel,Trapero Ana,Egido-Gabás Meritxell,Llebaria Amadeu,García Fernández José M.,Ortiz Mellet Carmen

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2011/OB/C1OB05234A

Reference49 articles.

1. Iminosugars: from botanical curiosities to licensed drugs

2. Recent Insights into Inhibition, Structure, and Mechanism of Configuration-Retaining Glycosidases

3. 1-Aza Sugars, Apparent Transition State Analogues of Equatorial Glycoside Formation/Cleavage

4. Glycoside Hydrolases: Mechanistic Information from Studies with Reversible and Irreversible Inhibitors

5. Design and evaluation of oral bioadhesive controlled release formulations of miglitol, intended for prolonged inhibition of intestinal α-glucosidases and enhancement of plasma glucagon like peptide-1 levels☆

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